CRSP vs EDIT Stock Comparison: AI Score, Valuation, Performance and Upside
CRSP is the clear leader in the CRISPR gene editing space having achieved the first-ever CRISPR therapy approval (Casgevy) with Vertex Pharmaceuticals, while EDIT is an earlier-stage gene editing company with clinical programs still working toward proving its approach. Both face the broader challenges of gene therapy commercialization, but CRSP has a meaningful head start.
CRSP vs EDIT compares the leading CRISPR gene editing company with a commercially approved therapy against an earlier-stage CRISPR competitor still advancing programs through clinical development.
CRSP holds the edge across 3 of 5 key metrics in this comparison. CRSP leads on both 1-year return (+21.74%) and forward P/E (-14.12x vs -2.87x for EDIT), a relatively favorable combination of momentum and valuation. Analyst consensus implies meaningfully more upside for EDIT (+114.79%) than for CRSP (+54.42%).
- →Want exposure to the gene editing company that achieved the first CRISPR therapy approval
- →Value the Vertex partnership for financial backing and commercial infrastructure
- →Believe CRISPR-based cures will build into meaningful commercial franchises
- →Want earlier-stage exposure to in vivo CRISPR gene editing technology
- →See potential value in Editas's foundational IP and clinical programs at a smaller valuation
- →Are comfortable with higher clinical and execution risk in exchange for earlier-stage upside
| Metric | CRSP | EDIT |
|---|---|---|
| AI score | 34.4 | 24.5 |
| AI rank | #1740 | #3100 |
| Latest close | $54.09 | $2.69 |
| 1M return | +13.66% | +9.35% |
| 6M return | -1.19% | +13.50% |
| 1Y return | +21.74% | +14.47% |
How much would $10,000 be worth today if invested at the start of each period, with all dividends reinvested?
| Period | CRSP | EDIT |
|---|---|---|
| 1Y ago | $12.17K (+21.7%) started 2025-06-18 | $11.45K (+14.5%) started 2025-06-18 |
| 5Y ago | $4.23K (-57.7%) started 2021-06-18 | $749.72 (-92.5%) started 2021-06-18 |
| 10Y ago | $38.39K (+283.9%) started 2016-10-19 | $906.33 (-90.9%) started 2016-06-20 |
Hypothetical — past performance does not guarantee future results.
| Metric | CRSP | EDIT |
|---|---|---|
| Market cap | $5.33B | $412.81M |
| Trailing P/E | N/A | N/A |
| Forward P/E | -14.12 | -2.87 |
| Price/Sales | 1298.32 | 10.67 |
| EV/Revenue | 819.67 | 3.22 |
| Analyst target | $83.52 | $5.78 |
| Target upside | +54.42% | +114.79% |
| Metric | CRSP | EDIT |
|---|---|---|
| Revenue growth | 68.60% | -39.20% |
| Earnings growth | N/A | N/A |
| EPS growth | N/A | N/A |
| FCF margin | -6358.66% | -190.77% |
| Operating margin | N/A | N/A |
| Profit margin | 0.00% | -281.59% |
| ROIC proxy | -31.21% | -326.07% |
| Return on equity | -31.21% | -326.07% |
| Dividend yield | 0.00% | 0.00% |
| Beta | 1.70 | 2.10 |
| Debt/equity | 43.41 | 392.40 |
| Current ratio | 17.96 | 3.22 |
| Quick ratio | 17.92 | 3.17 |
Lower drawdown and smaller single-period drops generally indicate a smoother ride, though they do not guarantee lower future risk.
| Period | Metric | CRSP | EDIT |
|---|---|---|---|
| 1Y | Growth | +21.74% | +14.47% |
| CAGR | +21.76% | +14.48% | |
| Sharpe ratio | 0.55 | 0.55 | |
| Max drawdown | 42.25% | 59.88% | |
| Max daily drop | 11.59% | 15.57% | |
| Max wkly drop | 17.63% | 27.17% | |
| 5Y | Growth | -57.69% | -92.50% |
| CAGR | -15.80% | -40.44% | |
| Sharpe ratio | -0.06 | -0.16 | |
| Max drawdown | 80.68% | 98.66% | |
| Max daily drop | 13.32% | 35.63% | |
| Max wkly drop | 21.49% | 42.50% | |
| 10Y | Growth | +283.89% | -90.94% |
| CAGR | +14.94% | -21.36% | |
| Sharpe ratio | 0.46 | 0.06 | |
| Max drawdown | 85.11% | 98.92% | |
| Max daily drop | 17.10% | 35.63% | |
| Max wkly drop | 30.47% | 42.50% |
| Category | CRSP | EDIT |
|---|---|---|
| Company | CRISPR Therapeutics AG | Editas Medicine, Inc. |
| Sector | Health Care - Gene Editing | Health Care - Gene Editing |
| Industry | N/A | N/A |
| Core business | CRISPR Therapeutics uses CRISPR-Cas9 gene editing to develop transformative medicines, led by Casgevy (exa-cel), the first CRISPR-based therapy approved by the FDA — for sickle cell disease and beta-thalassemia — developed in partnership with Vertex Pharmaceuticals. | Editas Medicine is a clinical-stage gene editing company using CRISPR-Cas9 and other gene editing tools to develop medicines, with early programs in eye disease (Leber congenital amaurosis) and hematological conditions. |
| Investor focus | Investors track Casgevy's commercial launch and patient uptake, the next wave of in vivo CRISPR programs (particularly cardiovascular), and the overall expansion of the gene editing therapy pipeline. | Investors track Editas's clinical pipeline advancement, particularly its in vivo eye disease programs, and the company's strategic focus following earlier setbacks and pipeline restructuring. |
- →First company to achieve FDA approval for a CRISPR-based therapy (Casgevy for sickle cell disease and beta-thalassemia)
- →Partnership with Vertex Pharmaceuticals provides commercial infrastructure and significant financial backing
- →Strong cash position from Vertex partnership funding enables substantial R&D investment
- →Early-mover in CRISPR gene editing with foundational IP positions
- →In vivo gene editing approach (delivering CRISPR directly into the body) could be simpler to administer than ex vivo approaches if successful
- →Eye disease programs provide early clinical proof-of-concept opportunities
- →Casgevy's commercial uptake has been limited by complex manufacturing, treatment requirements (patient conditioning), and high price — adoption is slower than initially hoped
- →Ex vivo gene editing approach requires complex bone marrow transplantation-like procedures that limit eligible patient numbers
- →Competition from other gene therapies including Bluebird Bio's Lyfgenia
- →No commercially approved therapies yet; all programs are pre-commercial
- →Has faced clinical and operational setbacks that required pipeline restructuring
- →Significantly smaller than CRISPR Therapeutics in both resources and clinical advancement
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